Table 1.

Patient characteristics

Prebiotics group (n = 49)Historical control group (n = 142)P
Sex   .179 
 Male 24 (49) 87 (61)  
 Female 25 (51) 55 (39)  
Age, y   .235 
 <55 34 (69) 84 (59)  
 ≥55 15 (31) 58 (41)  
Primary disease   .217 
 AML 25 (51) 70 (49)  
 ALL 10 (20) 25 (18)  
 MDS 4 (8) 28 (20)  
 Others 10 (20) 19 (13)  
Disease risk*   .250 
 Low risk 28 (57) 67 (47)  
 High risk 21 (43 75 (53)  
No. of transplantations   .803 
 1 44 (90) 123 (87)  
 ≥2 5 (10) 19 (13)  
Donor sex   .216 
 Male 37 (76) 92 (65)  
 Female 12 (24) 50 (35)  
Donor-recipient sex   .028 
 Female to male 2 (4) 24 (17)  
 Others 47 (96) 118 (83)  
HLA disparity (X/6)   .295 
 0 19 (39) 66 (46)  
 1 14 (29) 40 (28)  
 2 9 (18) 12 (8)  
 ≥3 7 (14) 24 (17)  
Allo-HSCT type   .309 
 rPBSCT 6 (12) 18 (13)  
 rBMT 2 (4) 3 (2)  
 uPBSCT 0 (0) 2 (1)  
 uBMT 21 (43) 77 (54)  
 CBT 8 (16) 15 (11)  
 Haplo (PT-CY) 6 (12) 6 (4)  
 Haplo (ATG+steroid) 6 (12) 21 (15)  
Conditioning   .095 
 MAC 33 (67) 75 (53)  
 RIC 16 (33) 67 (47)  
ATG   .819 
 Yes 8 (16) 21 (15)  
 No 41 (84) 121 (85)  
TBI   .522 
 Yes 42 (86) 115 (81)  
 No 7 (14) 27 (19)  
GVHD prophylaxis   .665 
 CsA-based 10 (20) 24 (17)  
 FK-based 39 (80) 118 (83)  
Use of antibiotics with relatively high anti-anaerobe activity (from conditioning to day 28)   <.001 
 None 13 (27) 25 (18)  
 1 line 26 (53) 110 (73)  
 2 lines 10 (20) 6 (4)  
Prebiotics group (n = 49)Historical control group (n = 142)P
Sex   .179 
 Male 24 (49) 87 (61)  
 Female 25 (51) 55 (39)  
Age, y   .235 
 <55 34 (69) 84 (59)  
 ≥55 15 (31) 58 (41)  
Primary disease   .217 
 AML 25 (51) 70 (49)  
 ALL 10 (20) 25 (18)  
 MDS 4 (8) 28 (20)  
 Others 10 (20) 19 (13)  
Disease risk*   .250 
 Low risk 28 (57) 67 (47)  
 High risk 21 (43 75 (53)  
No. of transplantations   .803 
 1 44 (90) 123 (87)  
 ≥2 5 (10) 19 (13)  
Donor sex   .216 
 Male 37 (76) 92 (65)  
 Female 12 (24) 50 (35)  
Donor-recipient sex   .028 
 Female to male 2 (4) 24 (17)  
 Others 47 (96) 118 (83)  
HLA disparity (X/6)   .295 
 0 19 (39) 66 (46)  
 1 14 (29) 40 (28)  
 2 9 (18) 12 (8)  
 ≥3 7 (14) 24 (17)  
Allo-HSCT type   .309 
 rPBSCT 6 (12) 18 (13)  
 rBMT 2 (4) 3 (2)  
 uPBSCT 0 (0) 2 (1)  
 uBMT 21 (43) 77 (54)  
 CBT 8 (16) 15 (11)  
 Haplo (PT-CY) 6 (12) 6 (4)  
 Haplo (ATG+steroid) 6 (12) 21 (15)  
Conditioning   .095 
 MAC 33 (67) 75 (53)  
 RIC 16 (33) 67 (47)  
ATG   .819 
 Yes 8 (16) 21 (15)  
 No 41 (84) 121 (85)  
TBI   .522 
 Yes 42 (86) 115 (81)  
 No 7 (14) 27 (19)  
GVHD prophylaxis   .665 
 CsA-based 10 (20) 24 (17)  
 FK-based 39 (80) 118 (83)  
Use of antibiotics with relatively high anti-anaerobe activity (from conditioning to day 28)   <.001 
 None 13 (27) 25 (18)  
 1 line 26 (53) 110 (73)  
 2 lines 10 (20) 6 (4)  

Data are expressed as number of patients (percentage of subgroup).

ALL, acute lymphoblastic leukemia; ATG, antithymocyte globulin; BMT, bone marrow transplantation; CBT, cord blood transplantation; CsA, cyclosporine; Haplo, haploidentical transplantation; MAC, myeloablative conditioning; MDS, myelodysplastic syndrome; PT-CY, posttransplantation cyclophosphamide; RIC, reduced-intensity conditioning; rPBSCT, related peripheral blood stem cell transplantation; uPBSCT, unrelated PBSCT.

*

Low-risk disease included acute leukemia in the first complete remission (CR), ronic myeloid leukemia (CML) in the first chronic phase, MDS in refractory anemia, malignant lymphoma in CR, and nonmalignant hematologic diseases. All other diagnoses and second allo-HSCT were included in high-risk disease.

Antibiotics with relatively high antianaerobic activity: meropenem, imipenem-cilastatin, and piperacillin-tazobactam. The other antibiotics were third- and fourth-generation cephems, polypeptides, quinolones, sulfamethoxazole-trimethoprim, aminoglycosides, and aztreonam.

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